Storey J R, Calder C S, Hart D E, Potter D L
Upstate Neurology Consultants, Albany, NY, USA.
Headache. 2001 Nov-Dec;41(10):968-75. doi: 10.1046/j.1526-4610.2001.01190.x.
To evaluate the efficacy of topiramate in the preventative treatment of episodic migraine.
Topiramate is a broad-spectrum antiepileptic drug effective for treatment of multiple seizure types in adults and children. Antiepileptic agents have demonstrated efficacy in migraine prevention, and open-label experience from our clinic has suggested that topiramate might be effective for this use. We consequently conducted a single-center, double-blind, placebo-controlled trial to evaluate the efficacy and safety of topiramate for the preventative treatment of migraine.
Forty patients, aged 19 to 62 years (mean, 38.2 years), were randomly assigned in a 1:1 ratio to receive topiramate (n = 19; all women) or placebo (n = 21; 20 women, 1 man). Following a prospective baseline phase of 4 weeks, the study drug dose was titrated weekly in 25-mg increments over 8 weeks to 200 mg per day or to the maximum tolerated dose. The titration phase was followed by an 8-week maintenance phase.
During the entire double-blind phase, topiramate-treated patients experienced a significantly lower 28-day migraine frequency (3.31 +/- 1.7 versus 3.83 +/- 2.1; P =.002) compared to placebo, irrespective of use of concomitant migraine prevention medications. The mean 28-day migraine frequency was reduced by 36% in patients receiving topiramate as compared with 14% in patients receiving placebo (P =.004). Twenty-six percent of the patients on topiramate and 9.5% of the patients on placebo achieved a 50% reduction in migraine frequency (P >.05). The mean dose of topiramate was 125 mg per day (range, 25 to 200 mg per day). Topiramate was well tolerated; 2 of 19 topiramate-treated patients discontinued treatment due to adverse events. Adverse effects that occurred more frequently in topiramate-treated patients included paresthesia, weight loss, altered taste, anorexia, and memory impairment.
Preventative therapy with topiramate significantly reduced migraine frequency. Larger multicenter clinical studies may further delineate the role of topiramate in migraine prevention.
评估托吡酯在发作性偏头痛预防性治疗中的疗效。
托吡酯是一种广谱抗癫痫药物,对成人和儿童的多种癫痫发作类型有效。抗癫痫药物已被证明在偏头痛预防中有效,我们诊所的开放标签经验表明托吡酯可能对此用途有效。因此,我们进行了一项单中心、双盲、安慰剂对照试验,以评估托吡酯预防性治疗偏头痛的疗效和安全性。
40名年龄在19至62岁(平均38.2岁)的患者按1:1比例随机分配,接受托吡酯(n = 19;均为女性)或安慰剂(n = 21;20名女性,1名男性)。在为期4周的前瞻性基线期后,研究药物剂量在8周内每周以25mg的增量滴定至每天200mg或最大耐受剂量。滴定期后是为期8周的维持期。
在整个双盲期,与安慰剂相比,托吡酯治疗的患者28天偏头痛发作频率显著更低(3.31±1.7对3.83±2.1;P = 0.002),无论是否使用偏头痛预防药物。接受托吡酯治疗的患者28天偏头痛平均发作频率降低了36%,而接受安慰剂治疗的患者降低了14%(P = 0.004)。26%服用托吡酯的患者和9.5%服用安慰剂的患者偏头痛发作频率降低了50%(P>0.05)。托吡酯的平均剂量为每天125mg(范围为每天25至200mg)。托吡酯耐受性良好;19名接受托吡酯治疗的患者中有2名因不良事件停药。托吡酯治疗患者中更频繁出现的不良反应包括感觉异常、体重减轻、味觉改变、厌食和记忆障碍。
托吡酯预防性治疗可显著降低偏头痛发作频率。更大规模的多中心临床研究可能会进一步明确托吡酯在偏头痛预防中的作用。